Elson Elliot L
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri, USA.
Methods Enzymol. 2013;518:11-41. doi: 10.1016/B978-0-12-388422-0.00002-9.
Fluorescence correlation spectroscopy (FCS) measures rates of transport (diffusion coefficients, convection velocities) and chemical reactions (rate constants) in equilibrium or nonequilibrium steady-state systems without the need for a perturbation of the state of the system. The rates are extracted from a record of fluorescence fluctuations observed from an open laser-illuminated observation volume. In addition, FCS provides the number of measured fluorescent molecules in the observation volume and, therefore, their molecular brightness. This enables sensitive measurements of aggregation of the fluorescent system components. FCS is now used as a routine tool for studying systems in physics, chemistry, and biology. Recent extensions of the fluorescence fluctuation approach have included methods based on imaging and cross correlation. Because of the sensitivity and chemical specificity of fluorescence detection and also the ability to form a very small diffraction-limited detection volume, FCS is especially useful for studies of dynamic molecular processes in living biological cells. FCS provides a window on mesoscopic systems and is closely related to fluorescence methods for studying single molecules.
荧光相关光谱法(FCS)可测量处于平衡态或非平衡稳态系统中的传输速率(扩散系数、对流速度)和化学反应速率(速率常数),而无需对系统状态进行扰动。这些速率是从开放激光照射观测体积中观察到的荧光涨落记录中提取出来的。此外,FCS可提供观测体积中被测荧光分子的数量,进而得出它们的分子亮度。这使得能够对荧光系统组分的聚集进行灵敏测量。FCS现在是研究物理、化学和生物学系统的常规工具。荧光涨落方法的最新扩展包括基于成像和互相关的方法。由于荧光检测的灵敏度和化学特异性,以及形成非常小的衍射极限检测体积的能力,FCS对于研究活生物细胞中的动态分子过程特别有用。FCS为介观系统提供了一个窗口,并且与研究单分子的荧光方法密切相关。